Canonical Allele Identifier: CA2695215388

Gene: PTS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112230588dup , CM000673.2:g.112230588dup	GRCh38
NC_000011.9:g.112101311dup , CM000673.1:g.112101311dup	GRCh37
NC_000011.8:g.111606521dup	NCBI36
NG_008743.1:g.9224dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000280362.8:c.187-38dup MANE Select	ENSP00000280362.3:n.187-38dup
ENST00000280362.7:c.187-38dup	ENSP00000280362.3:n.187-38dup
ENST00000524931.1:c.-18-38dup	ENSP00000434688.1:n.-18-38dup
ENST00000525803.1:c.163+1915dup	ENSP00000431750.1:n.163+1915dup
ENST00000527428.5:n.323dup
ENST00000527635.1:n.190dup
ENST00000528679.5:c.164-38dup	ENSP00000435895.1:n.164-38dup
ENST00000531175.1:n.138-38dup
ENST00000531673.5:c.164-38dup	ENSP00000433469.1:n.164-38dup
NM_000317.2:c.187-38dup	NP_000308.1:n.187-38dup
XM_011542943.1:c.148-38dup	XP_011541245.1:n.148-38dup
NM_000317.3:c.187-38dup MANE Select	NP_000308.1:n.187-38dup